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Randstad MQA Specialist I (Inspection) in Melrose Park, Illinois

MQA Specialist I (Inspection)

job details:

  • location:Melrose Park, IL

  • salary:$17 - $19.50 per hour

  • date posted:Monday, September 14, 2020

  • experience:3 Years

  • job type:Contract

  • industry:Professional, Scientific, and Technical Services

  • reference:33093

job description

MQA Specialist I (Inspection)

job summary:

As the world's largest staffing and recruitment agency in the world, we can commit to find you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. We supply prestigious life sciences and biopharma companies with job seekers like you to achieve their business goals. If you're looking for a position where you can serve as an asset to your company while making a difference in others' lives, we have the ideal position for you!

location: Melrose Park, Illinois

job type: Contract

salary: $17.00 - 19.50 per hour

work hours: 11 to 7

education: Bachelors

responsibilities:

  • Performs reviews of all operating processes and participates in internal quality assurance for the operations and facility. Will perform record reviews while on the production floor.

  • Recognizes opportunities for improvement and compliance and immediately communicates them to production colleagues and MQA Supervision. Directly participates in corrective actions of critical, major or minor deviations found.

  • Performs analysis of fill operations utilizing Statistical Process Control software.

  • Gown qualifies for Aseptic and Terminal Sterilization processes. Qualifies as a Visual Inspector for performing AQL inspections, subject to on-going qualification training/ testing.

  • Reviews manufacturing compounding of drug products for verification.

  • Assures line clearances and appropriate quality assurance procedures within the packaging areas.

  • Will be the cGMP "go to person" on the production floor.

  • Responsible to see that all operations on the production floor are being performed as required by written procedures and participates in the writing and approval of these procedures. Assures critical steps have been performed as directed in SOPs and batch records.

  • Demonstrates knowledge of production and support departments via the ability to perform, review and audit operations.

  • Assumes other duties as assigned.

qualifications:

  • BS in Life Sciences preferred or High School diploma with previous related field experience or knowledge of a GMP - regulated industry.

  • Minimum of High School Diploma with 3-5 years of related experience required.

  • Broad production knowledge a plus.

  • Computer knowledge a must. Knowledge of Word/Access and Excel applications a plus

skills: SOP, Quality Assurance, GMP (Good Manufacturing Practice)

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

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